Experience

AL HOTY STANGER LABORATORIES-UAE

• United Arab Emirates
• Consumer Services
• 100 - 200 Employee

• Chemist

  • Jun 2021 - Present

   Performed testing of portable water, wastewater, sea water, sludge and sediment samples  Documentation as per GMP and ISO guidelines  Establishment, documentation and implementation of Quality management System  Technical Operations- Method development & validation of analytical processes  Customer service and trouble shooting  Inventory Management  Training, Internal audits and participating in ISO audits  Management- Internal audits planning and execution… Show more  Performed testing of portable water, wastewater, sea water, sludge and sediment samples  Documentation as per GMP and ISO guidelines  Establishment, documentation and implementation of Quality management System  Technical Operations- Method development & validation of analytical processes  Customer service and trouble shooting  Inventory Management  Training, Internal audits and participating in ISO audits  Management- Internal audits planning and execution, report writing, recommending and follow up of corrective actions Show less  Performed testing of portable water, wastewater, sea water, sludge and sediment samples  Documentation as per GMP and ISO guidelines  Establishment, documentation and implementation of Quality management System  Technical Operations- Method development & validation of analytical processes  Customer service and trouble shooting  Inventory Management  Training, Internal audits and participating in ISO audits  Management- Internal audits planning and execution… Show more  Performed testing of portable water, wastewater, sea water, sludge and sediment samples  Documentation as per GMP and ISO guidelines  Establishment, documentation and implementation of Quality management System  Technical Operations- Method development & validation of analytical processes  Customer service and trouble shooting  Inventory Management  Training, Internal audits and participating in ISO audits  Management- Internal audits planning and execution, report writing, recommending and follow up of corrective actions Show less



Devayana Ayurvedic Medicines

• Palakkad, Kerala

• Quality Control Chemist

  • Jun 2018 - Feb 2021

   Analytical Method Development for Drug substance, drug Product and impurities  Preparation and finalization of trial drug formulations  Normal and accelerated stability studies according ICH and Pharmacoepial guidelines  Forced degradation/ stress tests for proposing degradation pathways  Identification of compounds using FTIR, NMR, HPLC, GC  Technical report writing and documentation  Routine wet chemistry and other chemical tests  Analysis and Interpretation … Show more  Analytical Method Development for Drug substance, drug Product and impurities  Preparation and finalization of trial drug formulations  Normal and accelerated stability studies according ICH and Pharmacoepial guidelines  Forced degradation/ stress tests for proposing degradation pathways  Identification of compounds using FTIR, NMR, HPLC, GC  Technical report writing and documentation  Routine wet chemistry and other chemical tests  Analysis and Interpretation  Pilot batch planning and execution and testing  Raw material and excipients testing and qualification  Designing and execution of experiments  Investigation and root cause analysis of deviations Show less  Analytical Method Development for Drug substance, drug Product and impurities  Preparation and finalization of trial drug formulations  Normal and accelerated stability studies according ICH and Pharmacoepial guidelines  Forced degradation/ stress tests for proposing degradation pathways  Identification of compounds using FTIR, NMR, HPLC, GC  Technical report writing and documentation  Routine wet chemistry and other chemical tests  Analysis and Interpretation … Show more  Analytical Method Development for Drug substance, drug Product and impurities  Preparation and finalization of trial drug formulations  Normal and accelerated stability studies according ICH and Pharmacoepial guidelines  Forced degradation/ stress tests for proposing degradation pathways  Identification of compounds using FTIR, NMR, HPLC, GC  Technical report writing and documentation  Routine wet chemistry and other chemical tests  Analysis and Interpretation  Pilot batch planning and execution and testing  Raw material and excipients testing and qualification  Designing and execution of experiments  Investigation and root cause analysis of deviations Show less



Bristol Laboratories Ltd.

• United Kingdom
• Pharmaceutical Manufacturing
• 300 - 400 Employee

• QC Laboratory Technician

  • Dec 2016 - Dec 2017

   Testing of Drug substances, Raw materials  Real time and accelerated degradability testing  HPLC- Purity and assay of Drug substance and impurity testing  Gas chromatography for impurity testing  Identification tests such as IR spectrum and comparison with standards  Sampling and documentation as per specifications  Documentation compliants with FDA and ISO specifications  Through understanding of SOPs ans written protocols  Experience in calibration and… Show more  Testing of Drug substances, Raw materials  Real time and accelerated degradability testing  HPLC- Purity and assay of Drug substance and impurity testing  Gas chromatography for impurity testing  Identification tests such as IR spectrum and comparison with standards  Sampling and documentation as per specifications  Documentation compliants with FDA and ISO specifications  Through understanding of SOPs ans written protocols  Experience in calibration and validation of instruments Show less  Testing of Drug substances, Raw materials  Real time and accelerated degradability testing  HPLC- Purity and assay of Drug substance and impurity testing  Gas chromatography for impurity testing  Identification tests such as IR spectrum and comparison with standards  Sampling and documentation as per specifications  Documentation compliants with FDA and ISO specifications  Through understanding of SOPs ans written protocols  Experience in calibration and… Show more  Testing of Drug substances, Raw materials  Real time and accelerated degradability testing  HPLC- Purity and assay of Drug substance and impurity testing  Gas chromatography for impurity testing  Identification tests such as IR spectrum and comparison with standards  Sampling and documentation as per specifications  Documentation compliants with FDA and ISO specifications  Through understanding of SOPs ans written protocols  Experience in calibration and validation of instruments Show less